-
1
-
-
0029057336
-
A single ataxia telangiectasia gene with a product similar to PI-3 kinase
-
Savitsky, K., Bar-Shira, A., Gilad, S., Rotman, G., Ziv, Y., Vanagaite, L., Tagle, D. A., Smith, S., Uziel, T., Sfez, S., Ashkenazi, M., Pecker, I., Frydman, M., Harnik, R., Patanjaki, S. R., Simmons, A., Clines, G. A., Sartiel, A., Gatti, R. A., Chessa, L., Sanal, O., Lavin, M. F., Jaspars, N. G. J., Taylor, A. M. R., Arlett, C. F., Miki, T., Weissman, S. M., Lovett, M., Collins, F. S., and Shiloh, Y. A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science (Wash. DC), 268: 1749-1753, 1995.
-
(1995)
Science (Wash. DC)
, vol.268
, pp. 1749-1753
-
-
Savitsky, K.1
Bar-Shira, A.2
Gilad, S.3
Rotman, G.4
Ziv, Y.5
Vanagaite, L.6
Tagle, D.A.7
Smith, S.8
Uziel, T.9
Sfez, S.10
Ashkenazi, M.11
Pecker, I.12
Frydman, M.13
Harnik, R.14
Patanjaki, S.R.15
Simmons, A.16
Clines, G.A.17
Sartiel, A.18
Gatti, R.A.19
Chessa, L.20
Sanal, O.21
Lavin, M.F.22
Jaspars, N.G.J.23
Taylor, A.M.R.24
Arlett, C.F.25
Miki, T.26
Weissman, S.M.27
Lovett, M.28
Collins, F.S.29
Shiloh, Y.30
more..
-
2
-
-
0037472924
-
DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation
-
Bakkenist, C. J., and Kastan, M. B. DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation. Nature (Lond.), 421: 499-506, 2003.
-
(2003)
Nature (Lond.)
, vol.421
, pp. 499-506
-
-
Bakkenist, C.J.1
Kastan, M.B.2
-
3
-
-
0037365789
-
ATM related protein kinases: Safeguarding genome integrity
-
Shiloh, Y. ATM and related protein kinases: safeguarding genome integrity. Nat. Rev. Cancer, 3: 155-168, 2003.
-
(2003)
Nat. Rev. Cancer
, vol.3
, pp. 155-168
-
-
Shiloh, Y.1
-
4
-
-
0022992181
-
The incidence and gene frequency of ataxia-telangiectasia in the United States
-
Swift, M., Morrell, D., Cromartie, E., Chamberlin, A. R., Skolnick, M. H., and Bishop, D. T. The incidence and gene frequency of ataxia-telangiectasia in the United States. Am. J. Hum. Genet., 39: 573-583, 1986.
-
(1986)
Am. J. Hum. Genet.
, vol.39
, pp. 573-583
-
-
Swift, M.1
Morrell, D.2
Cromartie, E.3
Chamberlin, A.R.4
Skolnick, M.H.5
Bishop, D.T.6
-
5
-
-
0025236412
-
Unusual features in the inheritance of ataxia telangiectasia
-
Woods, C. G., Bundey, S. E., and Taylor, A. M. Unusual features in the inheritance of ataxia telangiectasia. Hum. Genet., 84: 555-562, 1990.
-
(1990)
Hum. Genet.
, vol.84
, pp. 555-562
-
-
Woods, C.G.1
Bundey, S.E.2
Taylor, A.M.3
-
6
-
-
0034700243
-
Mortality rates among carriers of ataxia-telangiectasia mutant alleles
-
Su, Y., and Swift, M. Mortality rates among carriers of ataxia-telangiectasia mutant alleles. Ann. Intern. Med., 133: 770-778, 2000.
-
(2000)
Ann. Intern. Med.
, vol.133
, pp. 770-778
-
-
Su, Y.1
Swift, M.2
-
7
-
-
0028575693
-
Cancer risks in A-T heterozygotes
-
Easton, D. F. Cancer risks in A-T heterozygotes. Int. J. Radiat. Biol., 66: S177-S182, 1994.
-
(1994)
Int. J. Radiat. Biol.
, vol.66
-
-
Easton, D.F.1
-
8
-
-
0035879874
-
Cancer risk in heterozygotes for ataxia-telangiectasia
-
Geoffroy-Perez, B., Janin, N., Ossian, K., Lauge, A., Croquette, M. F., Griscelli, C., Debre, M., Bressac-de-Paillerets, B., Aurias, A., Stoppa-Lyonnet, D., and Andrieu, N. Cancer risk in heterozygotes for ataxia-telangiectasia. Int. J. Cancer, 93: 288-293, 2001.
-
(2001)
Int. J. Cancer
, vol.93
, pp. 288-293
-
-
Geoffroy-Perez, B.1
Janin, N.2
Ossian, K.3
Lauge, A.4
Croquette, M.F.5
Griscelli, C.6
Debre, M.7
Bressac-De-Paillerets, B.8
Aurias, A.9
Stoppa-Lyonnet, D.10
Andrieu, N.11
-
9
-
-
0032983665
-
Risk of breast cancer and other cancers in heterozygotes for ataxia- telangiectasia
-
Inskip, H. M., Kinlen, L. J., Taylor, A. M., Woods, C. G., and Arlett, C. F. Risk of breast cancer and other cancers in heterozygotes for ataxia- telangiectasia. Br. J. Cancer, 79: 1304-1307, 1999.
-
(1999)
Br. J. Cancer
, vol.79
, pp. 1304-1307
-
-
Inskip, H.M.1
Kinlen, L.J.2
Taylor, A.M.3
Woods, C.G.4
Arlett, C.F.5
-
10
-
-
0032926569
-
Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: Haplotype study in French AT families
-
Janin, N., Andrieu, N., Ossian, K., Lauge, A., Croquette, M. F., Griscelli, C., Debre, M., Bressac-de-Paillerets, B., Aurias, A., and Stoppa-Lyonnet, D. Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families. Br. J. Cancer, 80: 1042-1045, 1999.
-
(1999)
Br. J. Cancer
, vol.80
, pp. 1042-1045
-
-
Janin, N.1
Andrieu, N.2
Ossian, K.3
Lauge, A.4
Croquette, M.F.5
Griscelli, C.6
Debre, M.7
Bressac-De-Paillerets, B.8
Aurias, A.9
Stoppa-Lyonnet, D.10
-
11
-
-
0035900911
-
Cancer in patients with ataxia-telangiectasia and in their relatives in the Nordic countries
-
Olsen, J. H., Hahnemann, J. M., Borresen-Dale, A. L., Brondum-Nielsen, K., Hammarstrom, L., Kleinerman, R., Kaariainen, H., Lonnqvist, T., Sankila, R., Seersholm, N., Tretli, S., Yuen, J., Boice, J. D., and Tucker, M. Cancer in patients with ataxia-telangiectasia and in their relatives in the Nordic countries. J. Natl. Cancer Inst., 93: 121-127, 2001.
-
(2001)
J. Natl. Cancer Inst.
, vol.93
, pp. 121-127
-
-
Olsen, J.H.1
Hahnemann, J.M.2
Borresen-Dale, A.L.3
Brondum-Nielsen, K.4
Hammarstrom, L.5
Kleinerman, R.6
Kaariainen, H.7
Lonnqvist, T.8
Sankila, R.9
Seersholm, N.10
Tretli, S.11
Yuen, J.12
Boice, J.D.13
Tucker, M.14
-
12
-
-
0035166164
-
Screening breast cancer patients for ATM mutations and polymorphisms by using denaturing high-performance liquid chromatography
-
Atencio, D. P., Iannuzzi, C. M., Green, S., Stock, R. G., Bernstein, J. L., and Rosenstein, B. S. Screening breast cancer patients for ATM mutations and polymorphisms by using denaturing high-performance liquid chromatography. Environ. Mol. Mutagen., 38: 200-208, 2001.
-
(2001)
Environ. Mol. Mutagen.
, vol.38
, pp. 200-208
-
-
Atencio, D.P.1
Iannuzzi, C.M.2
Green, S.3
Stock, R.G.4
Bernstein, J.L.5
Rosenstein, B.S.6
-
13
-
-
0032756367
-
Identification of germline missense mutations and rare allelic variants in the ATM gene in early-onset breast cancer
-
Izatt, L., Greenman, J., Hodgson, S., Ellis, D., Watts, S., Scott, G., Jacobs, C., Liebmann, R., Zvelebil, M. J., Mathew, C., and Solomon, E. Identification of germline missense mutations and rare allelic variants in the ATM gene in early-onset breast cancer. Genes Chromosomes Cancer, 26: 286-294, 1999.
-
(1999)
Genes Chromosomes Cancer
, vol.26
, pp. 286-294
-
-
Izatt, L.1
Greenman, J.2
Hodgson, S.3
Ellis, D.4
Watts, S.5
Scott, G.6
Jacobs, C.7
Liebmann, R.8
Zvelebil, M.J.9
Mathew, C.10
Solomon, E.11
-
14
-
-
0035425350
-
Increased frequency of ATM mutations in breast carcinoma patients with early onset disease and positive family history
-
Teraoka, S. N., Malone, K. E., Doody, D. R., Suter, N. M., Ostrander, E. A., Daling, J. R., and Concannon, P. Increased frequency of ATM mutations in breast carcinoma patients with early onset disease and positive family history. Cancer (Phila.), 92: 479-487, 2001.
-
(2001)
Cancer (Phila.)
, vol.92
, pp. 479-487
-
-
Teraoka, S.N.1
Malone, K.E.2
Doody, D.R.3
Suter, N.M.4
Ostrander, E.A.5
Daling, J.R.6
Concannon, P.7
-
15
-
-
0035887491
-
Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patients
-
Dork, T., Bendix, R., Bremer, M., Rades, D., Klopper, K., Nicke, M., Skawran, B., Hector, A., Yamini, P., Steinmann, D., Weise, S., Stuhrmann, M., and Karstens, J. H. Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patients. Cancer Res., 61: 7608-7615, 2001.
-
(2001)
Cancer Res.
, vol.61
, pp. 7608-7615
-
-
Dork, T.1
Bendix, R.2
Bremer, M.3
Rades, D.4
Klopper, K.5
Nicke, M.6
Skawran, B.7
Hector, A.8
Yamini, P.9
Steinmann, D.10
Weise, S.11
Stuhrmann, M.12
Karstens, J.H.13
-
16
-
-
0036795006
-
Constitutional alterations of the ATM gene in early onset sporadic breast cancer
-
Maillet, P., Bonnefoi, H., Vaudan-Vutskits, G., Pajk, B., Cufer, T., Foulkes, W. D., Chappuis, P. O., and Sappino, A. P. Constitutional alterations of the ATM gene in early onset sporadic breast cancer. J. Med. Genet., 39: 751-753, 2002.
-
(2002)
J. Med. Genet.
, vol.39
, pp. 751-753
-
-
Maillet, P.1
Bonnefoi, H.2
Vaudan-Vutskits, G.3
Pajk, B.4
Cufer, T.5
Foulkes, W.D.6
Chappuis, P.O.7
Sappino, A.P.8
-
17
-
-
0033380655
-
Cancer risk in ATM heterozygotes: A model of phenotypic and mechanistic differences between missense and truncating mutations
-
Gatti, R. A., Tward, A., and Concannon, P. Cancer risk in ATM heterozygotes: a model of phenotypic and mechanistic differences between missense and truncating mutations. Mol. Genet. Metab., 68: 419-423, 1999.
-
(1999)
Mol. Genet. Metab.
, vol.68
, pp. 419-423
-
-
Gatti, R.A.1
Tward, A.2
Concannon, P.3
-
18
-
-
0036499132
-
ATM mutations in female breast cancer patients predict for an increase in radiation-induced late effects
-
Iannuzzi, C. M., Atencio, D. P., Green, S., Stock, R. G., and Rosenstein, B. S. ATM mutations in female breast cancer patients predict for an increase in radiation-induced late effects. Int. J. Radiat. Oncol. Biol. Phys., 52: 606-613, 2002.
-
(2002)
Int. J. Radiat. Oncol. Biol. Phys.
, vol.52
, pp. 606-613
-
-
Iannuzzi, C.M.1
Atencio, D.P.2
Green, S.3
Stock, R.G.4
Rosenstein, B.S.5
-
19
-
-
0032782760
-
Sequence analysis of the ATM gene in 20 patients with RTOG grade 3 or 4 acute and/or late tissue radiation side effects
-
Oppitz, U., Bernthaler, U., Schindler, D., Sobeck, A., Hoehn, H., Platzer, M., Rosenthal, A., and Flentje, M. Sequence analysis of the ATM gene in 20 patients with RTOG grade 3 or 4 acute and/or late tissue radiation side effects. Int. J. Radiat. Oncol. Biol. Phys., 44, 981-988, 1999.
-
(1999)
Int. J. Radiat. Oncol. Biol. Phys.
, vol.44
, pp. 981-988
-
-
Oppitz, U.1
Bernthaler, U.2
Schindler, D.3
Sobeck, A.4
Hoehn, H.5
Platzer, M.6
Rosenthal, A.7
Flentje, M.8
-
20
-
-
0030702833
-
Absence of mutations in the ATM gene in breast cancer patients with severe responses to radiotherapy
-
Appleby, J. M., Barber, J. B., Levine, E., Varley, J. M., Taylor, A. M., Stankovic, T., Heighway, J., Warren, C., and Scott, D. Absence of mutations in the ATM gene in breast cancer patients with severe responses to radiotherapy. Br. J. Cancer, 76: 1546-1549, 1997.
-
(1997)
Br. J. Cancer
, vol.76
, pp. 1546-1549
-
-
Appleby, J.M.1
Barber, J.B.2
Levine, E.3
Varley, J.M.4
Taylor, A.M.5
Stankovic, T.6
Heighway, J.7
Warren, C.8
Scott, D.9
-
21
-
-
0031803293
-
Testing for mutations of the ataxia telangiectasia gene in radiosensitive breast cancer patients
-
Ramsay, J., Birrell, G., and Lavin, M. Testing for mutations of the ataxia telangiectasia gene in radiosensitive breast cancer patients. Radiother. Oncol., 47: 125-128, 1998.
-
(1998)
Radiother. Oncol.
, vol.47
, pp. 125-128
-
-
Ramsay, J.1
Birrell, G.2
Lavin, M.3
-
22
-
-
7344226182
-
Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients
-
Shayeghi, M., Seal, S., Regan, J., Collins, N., Barfoot, R., Rahman, N., Ashton, A., Moohan, M., Wooster, R., Owen, R., Bliss, J. M., Stratton, M. R., and Yarnold, J. Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients. Br. J. Cancer, 78: 922-927, 1998.
-
(1998)
Br. J. Cancer
, vol.78
, pp. 922-927
-
-
Shayeghi, M.1
Seal, S.2
Regan, J.3
Collins, N.4
Barfoot, R.5
Rahman, N.6
Ashton, A.7
Moohan, M.8
Wooster, R.9
Owen, R.10
Bliss, J.M.11
Stratton, M.R.12
Yarnold, J.13
-
23
-
-
0032412555
-
Radiosensitivity of normal tissues in ataxia-telangiectasia heterozygotes
-
Weissberg, J. B., Huang, D. D., and Swift, M. Radiosensitivity of normal tissues in ataxia-telangiectasia heterozygotes. Int. J. Radiat. Oncol. Biol. Phys., 42: 1133-1136, 1998.
-
(1998)
Int. J. Radiat. Oncol. Biol. Phys.
, vol.42
, pp. 1133-1136
-
-
Weissberg, J.B.1
Huang, D.D.2
Swift, M.3
-
24
-
-
0031059354
-
Role of a 10-Gy boost in the conservative treatment of early breast cancer: Results of a randomized clinical trial in Lyon, France
-
Romestaing, P., Lehingue, Y., Carrie, C., Coquard, R., Montbarbon, X., Ardiet, J. M., Mamelle, N., and Gerard, J. P. Role of a 10-Gy boost in the conservative treatment of early breast cancer: results of a randomized clinical trial in Lyon, France. J. Clin. Oncol., 15: 963-968, 1997.
-
(1997)
J. Clin. Oncol.
, vol.15
, pp. 963-968
-
-
Romestaing, P.1
Lehingue, Y.2
Carrie, C.3
Coquard, R.4
Montbarbon, X.5
Ardiet, J.M.6
Mamelle, N.7
Gerard, J.P.8
-
25
-
-
0028969271
-
Toxicity criteria of the Radiation Therapy Oncology Group (RTOG) and the European Organization for Research and Treatment of Cancer (EORTC)
-
Cox, J. D., Stetz, J., and Pajak, T. F. Toxicity criteria of the Radiation Therapy Oncology Group (RTOG) and the European Organization for Research and Treatment of Cancer (EORTC). Int. J. Radiat. Oncol. Biol. Phys., 31: 1341-1346, 1995.
-
(1995)
Int. J. Radiat. Oncol. Biol. Phys.
, vol.31
, pp. 1341-1346
-
-
Cox, J.D.1
Stetz, J.2
Pajak, T.F.3
-
26
-
-
0037315580
-
Phenotypic cellular characterization of an ataxia telangiectasia patient carrying a causal homozygous missense mutation
-
Angèle, S., Lauge, A., Fernet, M., Moullan, N., Beauvais, P., Couturier, J., Stoppa-Lyonnet, D., and Hall, J. Phenotypic cellular characterization of an ataxia telangiectasia patient carrying a causal homozygous missense mutation. Hum. Mutat., 21: 169-170, 2003.
-
(2003)
Hum. Mutat.
, vol.21
, pp. 169-170
-
-
Angèle, S.1
Lauge, A.2
Fernet, M.3
Moullan, N.4
Beauvais, P.5
Couturier, J.6
Stoppa-Lyonnet, D.7
Hall, J.8
-
27
-
-
0037734244
-
Variation in radiation-induced apoptosis in ataxia telangiectasia lymphoblastoid cell line
-
Fernet, M., Angèle, S., Dork, T., and Hall, J. Variation in radiation-induced apoptosis in ataxia telangiectasia lymphoblastoid cell line. Int. J. Radiat. Biol., 79: 193-202, 2003.
-
(2003)
Int. J. Radiat. Biol.
, vol.79
, pp. 193-202
-
-
Fernet, M.1
Angèle, S.2
Dork, T.3
Hall, J.4
-
28
-
-
0029890959
-
Ataxia-telangiectasia: Mutations in ATM cDNA detected by protein-truncation screening
-
Telatar, M., Wang, Z., Udar, N., Liang, T., Bernatowska-Matuszkiewicz, E., Lavin, M., Shiloh, Y., Concannon, P., Good, R. A., and Gatti, R. A. Ataxia-telangiectasia: mutations in ATM cDNA detected by protein-truncation screening. Am. J. Hum. Genet., 59: 40-44, 1996.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 40-44
-
-
Telatar, M.1
Wang, Z.2
Udar, N.3
Liang, T.4
Bernatowska-Matuszkiewicz, E.5
Lavin, M.6
Shiloh, Y.7
Concannon, P.8
Good, R.A.9
Gatti, R.A.10
-
29
-
-
0042844840
-
Idiopathic and radiation induced ocular telangiectasias: The involvement of the ATM gene
-
Mauget-Faysse, M., Vuillaume, M., Quaranta, M., Moullan, N., Angèle, S., Friesen, M. D., and Hall, J. Idiopathic and radiation induced ocular telangiectasias: the involvement of the ATM gene. Investig. Ophthalmol. Vis. Sci., 44: 3257-3262, 2003.
-
(2003)
Investig. Ophthalmol. Vis. Sci.
, vol.44
, pp. 3257-3262
-
-
Mauget-Faysse, M.1
Vuillaume, M.2
Quaranta, M.3
Moullan, N.4
Angèle, S.5
Friesen, M.D.6
Hall, J.7
-
30
-
-
0032952338
-
Characterization of ATM gene mutations in 66 ataxia telangiectasia families
-
Sandoval, N., Platzer, M., Rosenthal, A., Dork, T., Bendix, R., Skawran, B., Stuhrmann, M., Wegner, R. D., Sperling, K., Banin, S., Shiloh, Y., Baumer, A., Bernthaler, U., Sennefelder, H., Brohm, M., Weber, B. H., and Schindler, D. Characterization of ATM gene mutations in 66 ataxia telangiectasia families. Hum. Mol. Genet., 8: 69-79, 1999.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 69-79
-
-
Sandoval, N.1
Platzer, M.2
Rosenthal, A.3
Dork, T.4
Bendix, R.5
Skawran, B.6
Stuhrmann, M.7
Wegner, R.D.8
Sperling, K.9
Banin, S.10
Shiloh, Y.11
Baumer, A.12
Bernthaler, U.13
Sennefelder, H.14
Brohm, M.15
Weber, B.H.16
Schindler, D.17
-
31
-
-
0033082846
-
PCR-mediated detection of a polymorphism in the ATM gene
-
Maillet, P., Vaudan, G., Chappuis, P., and Sappino, A. PCR-mediated detection of a polymorphism in the ATM gene. Mol. Cell. Probes, 13: 67-69, 1999.
-
(1999)
Mol. Cell. Probes
, vol.13
, pp. 67-69
-
-
Maillet, P.1
Vaudan, G.2
Chappuis, P.3
Sappino, A.4
-
32
-
-
0034854993
-
Genotype transposer: Automated genotype manipulation for linkage disequilibrium analysis
-
Cox, D. G., and Canzian, F. Genotype transposer: automated genotype manipulation for linkage disequilibrium analysis. Bioinformatics, 17: 738-739, 2001.
-
(2001)
Bioinformatics
, vol.17
, pp. 738-739
-
-
Cox, D.G.1
Canzian, F.2
-
34
-
-
0031711843
-
The p53-mediated DNA damage response to ionizing radiation in fibroblasts from ataxia-without-telangiectasia patients
-
Jongmans, W., Vuillaume, M., Kleijer, W. J., Lakin, N. D., and Hall, J. The p53-mediated DNA damage response to ionizing radiation in fibroblasts from ataxia-without-telangiectasia patients. Int. J. Radiat. Biol., 74: 287-295, 1998.
-
(1998)
Int. J. Radiat. Biol.
, vol.74
, pp. 287-295
-
-
Jongmans, W.1
Vuillaume, M.2
Kleijer, W.J.3
Lakin, N.D.4
Hall, J.5
-
35
-
-
17344370225
-
Genotype-phenotype relationships in ataxia-telangiectasia and variants
-
Gilad, S., Chessa, L., Khosravi, R., Russell, P., Galanty, Y., Piane, M., Gatti, R. A., Jorgensen, T. J., Shiloh, Y., and Bar-Shira, A. Genotype-phenotype relationships in ataxia-telangiectasia and variants. Am. J. Hum. Genet., 62: 551-561, 1998.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 551-561
-
-
Gilad, S.1
Chessa, L.2
Khosravi, R.3
Russell, P.4
Galanty, Y.5
Piane, M.6
Gatti, R.A.7
Jorgensen, T.J.8
Shiloh, Y.9
Bar-Shira, A.10
-
36
-
-
0029808695
-
The role of Ataxia telangiectasia and the DNA-dependent protein kinase in the p53-mediated cellular response to ionising radiation
-
Jongmans, W., Artuso, M., Vuillaume, M., Bresil, H., Jackson, S. P., and Hall, J. The role of Ataxia telangiectasia and the DNA-dependent protein kinase in the p53-mediated cellular response to ionising radiation. Oncogene, 13: 1133-1138, 1996.
-
(1996)
Oncogene
, vol.13
, pp. 1133-1138
-
-
Jongmans, W.1
Artuso, M.2
Vuillaume, M.3
Bresil, H.4
Jackson, S.P.5
Hall, J.6
-
37
-
-
0033911566
-
ATM-heterozygous germline mutations contribute to breast cancer-susceptibility
-
Broeks, A., Urbanus, J. H., Floore, A. N., Dahler, E. C., Klijn, J. G., Rutgers, E. J., Devilee, P., Russell, N. S., van Leeuwen, F. E., and van't Veer, L. J. ATM-heterozygous germline mutations contribute to breast cancer-susceptibility. Am. J. Hum. Genet., 66: 494-500, 2000.
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 494-500
-
-
Broeks, A.1
Urbanus, J.H.2
Floore, A.N.3
Dahler, E.C.4
Klijn, J.G.5
Rutgers, E.J.6
Devilee, P.7
Russell, N.S.8
Van Leeuwen, F.E.9
Van't Veer, L.J.10
-
38
-
-
0037028740
-
Dominant negative ATM mutations in breast cancer families
-
Chenevix-Trench, G., Spurdle, A. B., Gatei, M., Kelly, H., Marsh, A., Chen, X., Donn, K., Cummings, M., Nyholt, D., Jenkins, M. A., Scott, C., Pupo, G. M., Dork, T., Bendix, R., Kirk, J., Tucker, K., McCredie, M. R., Hopper, J. L., Sambrook, J., Mann, G. J., and Khanna, K. K. Dominant negative ATM mutations in breast cancer families. J. Natl. Cancer Inst., 94: 205-215, 2002.
-
(2002)
J. Natl. Cancer Inst.
, vol.94
, pp. 205-215
-
-
Chenevix-Trench, G.1
Spurdle, A.B.2
Gatei, M.3
Kelly, H.4
Marsh, A.5
Chen, X.6
Donn, K.7
Cummings, M.8
Nyholt, D.9
Jenkins, M.A.10
Scott, C.11
Pupo, G.M.12
Dork, T.13
Bendix, R.14
Kirk, J.15
Tucker, K.16
McCredie, M.R.17
Hopper, J.L.18
Sambrook, J.19
Mann, G.J.20
Khanna, K.K.21
more..
-
39
-
-
17344362697
-
ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: Expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer
-
Stankovic, T., Kidd, A. M., Sutcliffe, A., McGuire, G. M., Robinson, P., Weber, P., Bedenham, T., Bradwell, A. R., Easton, D. F., Lennox, G. G., Haites, N., Byrd, P. J., and Taylor, A. M. ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer. Am. J. Hum. Genet., 62: 334-345, 1998.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 334-345
-
-
Stankovic, T.1
Kidd, A.M.2
Sutcliffe, A.3
McGuire, G.M.4
Robinson, P.5
Weber, P.6
Bedenham, T.7
Bradwell, A.R.8
Easton, D.F.9
Lennox, G.G.10
Haites, N.11
Byrd, P.J.12
Taylor, A.M.13
-
40
-
-
0026496885
-
A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia
-
Kastan, M. B., Zhan, Q., el Deiry, W. S., Carrier, F., Jacks, T., Walsh, W. V., Plunkett, B. S., Vogelstein, B., and Fornace, A. J., Jr. A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia. Cell, 71: 587-597, 1992.
-
(1992)
Cell
, vol.71
, pp. 587-597
-
-
Kastan, M.B.1
Zhan, Q.2
El Deiry, W.S.3
Carrier, F.4
Jacks, T.5
Walsh, W.V.6
Plunkett, B.S.7
Vogelstein, B.8
Fornace Jr., A.J.9
-
41
-
-
0028788337
-
The role of the Ataxia telangiectasia gene in the p53, WAF1/CIP1(p21)- and GADD45-mediated response to DNA damage produced by ionising radiation
-
Artuso, M., Esteve, A., Bresil, H., Vuillaume, M., and Hall, J. The role of the Ataxia telangiectasia gene in the p53, WAF1/CIP1(p21)- and GADD45-mediated response to DNA damage produced by ionising radiation. Oncogene, 11: 1427-1435, 1995.
-
(1995)
Oncogene
, vol.11
, pp. 1427-1435
-
-
Artuso, M.1
Esteve, A.2
Bresil, H.3
Vuillaume, M.4
Hall, J.5
-
42
-
-
0032778345
-
Absence of mutations in the ATM gene in forty-seven cases of sporadic breast cancer
-
Bebb, D. G., Yu, Z., Chen, J., Telatar, M., Gelmon, K., Phillips, N., Gatti, R. A., and Glickman, B. W. Absence of mutations in the ATM gene in forty-seven cases of sporadic breast cancer. Br. J. Cancer, 80: 1979-1981, 1999.
-
(1999)
Br. J. Cancer
, vol.80
, pp. 1979-1981
-
-
Bebb, D.G.1
Yu, Z.2
Chen, J.3
Telatar, M.4
Gelmon, K.5
Phillips, N.6
Gatti, R.A.7
Glickman, B.W.8
-
43
-
-
0031029676
-
Heterozygous ATM mutations do not contribute to early onset of breast cancer
-
FitzGerald, M. G., Bean, J. M., Hegde, S. R., Unsal, H., MacDonald, D. J., Harkin, D. P., Finkelstein, D. M., Isselbacher, K. J., and Haber, D. A. Heterozygous ATM mutations do not contribute to early onset of breast cancer. Nat. Genet., 15: 307-310, 1997.
-
(1997)
Nat. Genet.
, vol.15
, pp. 307-310
-
-
FitzGerald, M.G.1
Bean, J.M.2
Hegde, S.R.3
Unsal, H.4
MacDonald, D.J.5
Harkin, D.P.6
Finkelstein, D.M.7
Isselbacher, K.J.8
Haber, D.A.9
-
44
-
-
0037405914
-
IVS10-6T>G, an ancient ATM germline mutation linked with breast cancer
-
Broeks, A., Urbanus, J. H., de Knijff, P., Devilee, P., Nicke, M., Klopper, K., Dork, T., Floore, A. N., and van't Veer, L. J. IVS10-6T>G, an ancient ATM germline mutation linked with breast cancer. Hum. Mutat., 21: 521-528, 2003.
-
(2003)
Hum. Mutat.
, vol.21
, pp. 521-528
-
-
Broeks, A.1
Urbanus, J.H.2
De Knijff, P.3
Devilee, P.4
Nicke, M.5
Klopper, K.6
Dork, T.7
Floore, A.N.8
Van't Veer, L.J.9
-
45
-
-
0000520601
-
An allelic variant at the ATM locus is implicated in breast cancer susceptibility
-
Larson, G. P., Zhang, G., Ding, S., Foldenauer, K., Udar, N., Gatti, R. A., Neuberg, D., Lunetta, K. L., Ruckdeschel, J. C., Longmate, J., Flanagan, S., and Krontiris, T. G. An allelic variant at the ATM locus is implicated in breast cancer susceptibility. Genet. Test., 1: 165-170, 1997.
-
(1997)
Genet. Test.
, vol.1
, pp. 165-170
-
-
Larson, G.P.1
Zhang, G.2
Ding, S.3
Foldenauer, K.4
Udar, N.5
Gatti, R.A.6
Neuberg, D.7
Lunetta, K.L.8
Ruckdeschel, J.C.9
Longmate, J.10
Flanagan, S.11
Krontiris, T.G.12
-
46
-
-
18344366334
-
Elevated frequency of ATM gene missense mutations in breast cancer relative to ethnically matched controls
-
Sommer, S. S., Buzin, C. H., Jung, M., Zheng, J., Liu, Q., Jeong, S. J., Moulds, J., Nguyen, V. Q., Feng, J., Bennett, W. P., and Dritschilo, A. Elevated frequency of ATM gene missense mutations in breast cancer relative to ethnically matched controls. Cancer Genet. Cytogenet., 134: 25-32, 2002.
-
(2002)
Cancer Genet. Cytogenet.
, vol.134
, pp. 25-32
-
-
Sommer, S.S.1
Buzin, C.H.2
Jung, M.3
Zheng, J.4
Liu, Q.5
Jeong, S.J.6
Moulds, J.7
Nguyen, V.Q.8
Feng, J.9
Bennett, W.P.10
Dritschilo, A.11
-
47
-
-
34247625921
-
No evidence for association of ataxia-telangiectasia mutated gene T2119C and C3161G amino acid substitution variants with risk of breast cancer
-
Spurdle, A. B., Hopper, J. L., Chen, X., McCredie, M. R., Giles, G. G., Newman, B., Chenevix-Trench, G., and Khanna, K. No evidence for association of ataxia-telangiectasia mutated gene T2119C and C3161G amino acid substitution variants with risk of breast cancer. Breast Cancer Res., 4: R15, 2002.
-
(2002)
Breast Cancer Res.
, vol.4
-
-
Spurdle, A.B.1
Hopper, J.L.2
Chen, X.3
McCredie, M.R.4
Giles, G.G.5
Newman, B.6
Chenevix-Trench, G.7
Khanna, K.8
-
48
-
-
0036606622
-
Effect of germ-line genetic variation on breast cancer survival in a population-based study
-
Goode, E. L., Dunning, A. M., Kuschel, B., Healey, C. S., Day, N. E., Ponder, B. A., Easton, D. F., and Pharoah, P. P. Effect of germ-line genetic variation on breast cancer survival in a population-based study. Cancer Res., 62: 3052-3057, 2002.
-
(2002)
Cancer Res.
, vol.62
, pp. 3052-3057
-
-
Goode, E.L.1
Dunning, A.M.2
Kuschel, B.3
Healey, C.S.4
Day, N.E.5
Ponder, B.A.6
Easton, D.F.7
Pharoah, P.P.8
-
49
-
-
0001019579
-
Breast cancer
-
D. Schottenfeld and J. F. Fraumeni (eds.). New York: Oxford University Press
-
Henderson, B. E., Pike, M. C., Bernstein L., Ross, R. K. Breast cancer. In: D. Schottenfeld and J. F. Fraumeni (eds.), Cancer Epidemiology and Prevention, pp. 1022-1039. New York: Oxford University Press, 1996.
-
(1996)
Cancer Epidemiology and Prevention
, pp. 1022-1039
-
-
Henderson, B.E.1
Pike, M.C.2
Bernstein, L.3
Ross, R.K.4
-
50
-
-
0037154221
-
Missense mutations but not allelic variants alter the function of ATM by dominant interference in patients with breast cancer
-
Scott, S. P., Bendix, R., Chen, P., Clark, R., Dork, T., and Lavin, M. F. Missense mutations but not allelic variants alter the function of ATM by dominant interference in patients with breast cancer. Proc. Natl. Acad. Sci. USA, 99: 925-930, 2002.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 925-930
-
-
Scott, S.P.1
Bendix, R.2
Chen, P.3
Clark, R.4
Dork, T.5
Lavin, M.F.6
-
51
-
-
0033658948
-
Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium
-
Bonnen, P. E., Story, M. D., Ashorn, C. L., Buchholz, T. A., Weil, M. M., and Nelson, D. L. Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium. Am. J. Hum. Genet., 67: 1437-1451, 2000.
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 1437-1451
-
-
Bonnen, P.E.1
Story, M.D.2
Ashorn, C.L.3
Buchholz, T.A.4
Weil, M.M.5
Nelson, D.L.6
-
52
-
-
0035112692
-
Polymorphic variation in CYP19 and the risk of breast cancer
-
Baxter, S. W., Choong, D. Y., Eccles, D. M., and Campbell, I. G. Polymorphic variation in CYP19 and the risk of breast cancer. Carcinogenesis (Lond.), 22: 347-349, 2001.
-
(2001)
Carcinogenesis (Lond.)
, vol.22
, pp. 347-349
-
-
Baxter, S.W.1
Choong, D.Y.2
Eccles, D.M.3
Campbell, I.G.4
-
53
-
-
0034662307
-
A tetranucleotide repeat polymorphism in CYP19 and breast cancer risk
-
Haiman, C. A., Hankinson, S. E., Spiegelman, D., De Vivo, I., Colditz, G. A., Willett, W. C., Speizer, F. E., and Hunter, D. J. A tetranucleotide repeat polymorphism in CYP19 and breast cancer risk. Int. J. Cancer, 87: 204-210, 2000.
-
(2000)
Int. J. Cancer
, vol.87
, pp. 204-210
-
-
Haiman, C.A.1
Hankinson, S.E.2
Spiegelman, D.3
De Vivo, I.4
Colditz, G.A.5
Willett, W.C.6
Speizer, F.E.7
Hunter, D.J.8
-
54
-
-
0036125699
-
Associations between common polymorphisms in TP53 and p21WAF1/Cip1 and phenotypic features of breast cancer
-
Powell, B. L., van Staveren, I. L., Roosken, P., Grieu, F., Berns, E. M., and Iacopetta, B. Associations between common polymorphisms in TP53 and p21WAF1/Cip1 and phenotypic features of breast cancer. Carcinogenesis (Lond.), 23: 311-315, 2002.
-
(2002)
Carcinogenesis (Lond.)
, vol.23
, pp. 311-315
-
-
Powell, B.L.1
Van Staveren, I.L.2
Roosken, P.3
Grieu, F.4
Berns, E.M.5
Iacopetta, B.6
-
55
-
-
0038402756
-
Acute toxicity of concurrent adjuvant radiotherapy and chemotherapy (CMF or AC) in breast cancer patients: A prospective, comparative, non-randomised study
-
Fiets, W. E., van Helvoit, R. P., Nortier, J. W. R., van der Tweel, I., and Struikmans, H. Acute toxicity of concurrent adjuvant radiotherapy and chemotherapy (CMF or AC) in breast cancer patients: a prospective, comparative, non-randomised study. Eur. J. Cancer, 39: 1081-1088, 2003.
-
(2003)
Eur. J. Cancer
, vol.39
, pp. 1081-1088
-
-
Fiets, W.E.1
Van Helvoit, R.P.2
Nortier, J.W.R.3
Van Der Tweel, I.4
Struikmans, H.5
-
56
-
-
0031738103
-
A preliminary report: Frequency of A-T heterozygotes among prostate cancer patients with severe late responses to radiation therapy
-
Hall, E. J., Schiff, P. B., Hanks, G. E., Brenner, D. J., Russo, J., Chen, J., Sawant, S. G., and Pandita, T. K. A preliminary report: frequency of A-T heterozygotes among prostate cancer patients with severe late responses to radiation therapy. Cancer J. Sci. Am., 4: 385-389, 1998.
-
(1998)
Cancer J. Sci. Am.
, vol.4
, pp. 385-389
-
-
Hall, E.J.1
Schiff, P.B.2
Hanks, G.E.3
Brenner, D.J.4
Russo, J.5
Chen, J.6
Sawant, S.G.7
Pandita, T.K.8
-
57
-
-
0034672288
-
A polymorphism in the ATM gene modulates the penetrance of hereditary non-polyposis colorectal cancer
-
Maillet, P., Chappuis, P. O., Vaudan, G., Dobbie, Z., Muller, H., Hutter, P., and Sappino, A. P. A polymorphism in the ATM gene modulates the penetrance of hereditary non-polyposis colorectal cancer. Int. J. Cancer, 88: 928-931, 2000.
-
(2000)
Int. J. Cancer
, vol.88
, pp. 928-931
-
-
Maillet, P.1
Chappuis, P.O.2
Vaudan, G.3
Dobbie, Z.4
Muller, H.5
Hutter, P.6
Sappino, A.P.7
-
58
-
-
0030893288
-
Radiation protection of radiosensitive populations
-
Mossman, K. L. Radiation protection of radiosensitive populations. Health Phys., 72: 519-523, 1997.
-
(1997)
Health Phys.
, vol.72
, pp. 519-523
-
-
Mossman, K.L.1
-
59
-
-
0031737611
-
Describing patients' normal tissue reactions: Concerning the possibility of individualising radiotherapy dose prescripfions based on potential predictive assays of normal tissue radiosensitivity
-
Steering Committee of the BioMed2 European Union Concerted Action Programme on the Development of Predictive Tests of Normal Tissue Response to Radiation Therapy
-
Burnet, N. G., Johansen, J., Turesson, I., Nyman, J., and Peacock, J. H. Describing patients' normal tissue reactions: concerning the possibility of individualising radiotherapy dose prescripfions based on potential predictive assays of normal tissue radiosensitivity. Steering Committee of the BioMed2 European Union Concerted Action Programme on the Development of Predictive Tests of Normal Tissue Response to Radiation Therapy. Int. J. Cancer, 79: 606-613, 1998.
-
(1998)
Int. J. Cancer
, vol.79
, pp. 606-613
-
-
Burnet, N.G.1
Johansen, J.2
Turesson, I.3
Nyman, J.4
Peacock, J.H.5
-
60
-
-
0030474646
-
Prognostic factors for acute and late skin reactions in radiotherapy patients
-
Turesson, I., Nyman, J., Holmberg, E., and Oden, A. Prognostic factors for acute and late skin reactions in radiotherapy patients. Int. J. Radiat. Oncol. Biol. Phys., 36: 1065-1075, 1996.
-
(1996)
Int. J. Radiat. Oncol. Biol. Phys.
, vol.36
, pp. 1065-1075
-
-
Turesson, I.1
Nyman, J.2
Holmberg, E.3
Oden, A.4
-
61
-
-
0035424764
-
Novel DNA sequence variants in the hHR21 DNA repair gene in radiosensitive cancer patients
-
Severin, D. M., Leong, T., Cassidy, B., Elsaleh, H., Peters, L., Venter, D., Southey, M., and McKay, M. Novel DNA sequence variants in the hHR21 DNA repair gene in radiosensitive cancer patients. Int. J. Radiat. Oncol. Biol. Phys., 50: 1323-1331, 2001.
-
(2001)
Int. J. Radiat. Oncol. Biol. Phys.
, vol.50
, pp. 1323-1331
-
-
Severin, D.M.1
Leong, T.2
Cassidy, B.3
Elsaleh, H.4
Peters, L.5
Venter, D.6
Southey, M.7
McKay, M.8
-
62
-
-
0344198151
-
Polymorphisms in the DNA repair gene XRCC1, breast cancer risk and response to radiotherapy
-
in press
-
Moullan, N., Cox, D. G., Angèle, S., Romestaing, P., Gerard, J. P., and Hall, J. Polymorphisms in the DNA repair gene XRCC1, breast cancer risk and response to radiotherapy. Cancer Epidemiol. Biomark Prev., in press, 2003.
-
(2003)
Cancer Epidemiol. Biomark Prev.
-
-
Moullan, N.1
Cox, D.G.2
Angèle, S.3
Romestaing, P.4
Gerard, J.P.5
Hall, J.6
-
63
-
-
0034927535
-
Global analysis of ATM polymorphism reveals significant functional constraint
-
Thorstenson, Y. R., Shen, P., Tusher, V. G., Wayne, T. L., Davis, R. W., Chu, G., and Oefner, P. J. Global analysis of ATM polymorphism reveals significant functional constraint. Am. J. Hum. Genet., 69: 396-412, 2001.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 396-412
-
-
Thorstenson, Y.R.1
Shen, P.2
Tusher, V.G.3
Wayne, T.L.4
Davis, R.W.5
Chu, G.6
Oefner, P.J.7
-
64
-
-
0344562925
-
Neutral sequence variants and haplotypes at the 150 Kb ataxia-telangiectasia locus
-
Li, A., Huang, Y., and Swift, M. Neutral sequence variants and haplotypes at the 150 Kb ataxia-telangiectasia locus. Am. J. Med. Genet., 86: 140-144, 1999.
-
(1999)
Am. J. Med. Genet.
, vol.86
, pp. 140-144
-
-
Li, A.1
Huang, Y.2
Swift, M.3
|